pulmonaryfibrosis.org.uk
Pulmonary Fibrosis UKSite for those effected by the respiratory disease Pulmonary Fibrosis, including; suferers, family members, carers, doctors, nurses
http://pulmonaryfibrosis.org.uk/
Site for those effected by the respiratory disease Pulmonary Fibrosis, including; suferers, family members, carers, doctors, nurses
http://pulmonaryfibrosis.org.uk/
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Pulmonary Fibrosis UK | pulmonaryfibrosis.org.uk Reviews
https://pulmonaryfibrosis.org.uk
Site for those effected by the respiratory disease Pulmonary Fibrosis, including; suferers, family members, carers, doctors, nurses
Pulmonary Fibrosis Support Group - Links
http://www.pulmonaryfibrosis.org.nz/links
Pulmonary Fibrosis Support Group. Pulmonary Fibrosis Foundation (USA). UK Pulmonary Support Group. Canadian Pulmonary Fibrosis Foundation. Other resources NZ sufferers. Named Patient Pharmaceutical Assessment. Access to treatments that aren’t on the lists). The Roche Medical Information phone number is 0800 276 243. Pulmonary Fibrosis Support Group.
Irish Lung Fibrosis Association
http://www.ilfa.ie/useful_links.asp
News and Upcoming Events. 2000 Steps a Day exercise challenge. Tip of the Week 2016. Inspirational Quote of the Week. Follow Us on Facebook! News and Events archive. Song for Liam" CD. Would You Like To Become More Involved With ILFA? Perhaps you could do a once-off fundraising event such as a coffee morning or maybe you would be interested in setting up a local ILFA branch where you live. You can contact us via post @ PO Box 10456, Blackrock, County Dublin; via email @ info@ilfa.ie. The CPF funds promis...
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Pulmonary Fibrosis in India
Pulmonary Fibrosis in India Together we are stronger. An international roadtrip for IPF Awareness. Mon 27 July 2015. Breathe free, live free. Is an expedition being organized to raise IPF Awareness across China, Laos, Thailand, Burma, and India. The idea is to raise grassroots awareness for IPF through a roadtrip, by meeting people, distributing pamphlets, etc. You can donate to the cause at the first-giving page. All proceeds shall be donated to the Pulmonary Fibrosis Foundation. Sun 06 October 2013.
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Pulmonary Fibrosis Foundation | pulmonaryfibrosis.org
Fundraise for Team PFF. Shop at PFF Store. Honor a Loved One. Support PFF at Work. Broadway Belts for PFF. Donate Stocks and Bonds. Leanne Storch Support Group Fund. PFF Care Center Network. Join Our Monthly eNewsletter. Subscribe to receive the most current news and updates from the Pulmonary Fibrosis Foundation. Support Group Leader Network. Ask A Doc March 2015. PFF in the Media. PFF Care Center Network. Global PF Awareness Month. PFF Patient Communication Center. PFF Support Group Leader Network.
Pulmonary Fibrosis Support Group - Home
Pulmonary Fibrosis Support Group. When IPF Gets Worse. Coping with Terminal Illness. Welcome to the website of the Pulmonary Fibrosis Support Group. The mission statement for the PF Support Group is to provide a sympathetic environment for supporting people and their families/carers throughout the course of their disease. Provide an informative website,. Produce a pamphlet and a patient’s handbook,. Promote disease awareness in the community,. Lobby for more research into the disease,.
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